MedtechSourcebook

TRIDENT MANUFACTURING, INC.

Contract manufacturer ยท Pingree Grove, IL

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

2014Product codes first listed, by year (tallest: 3)2026
FDA registration
3008717566 (openFDA record; or search FDA's registration database)
FEI number
3008717566
Registered for
FDA registration year 2026
Establishment types
Manufacturer for export only; Contract manufacturer; Repackager or relabeler
Owner or operator
TRIDENT MANUFACTURING, INC. (FDA owner/operator no. 10029801)
Registered address
41W275 RAILROAD STREET, Pingree Grove, IL 60140
Contract listings
12 device listings, 10 product codes, first listed May 30, 2014
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
CBHDevice, Fixation, Tracheal TubeClass IAnesthesiologyContract manufacturingNov 22, 2021
DXCClamp, VascularClass IICardiovascularContract manufacturingDec 4, 2025
GEJCarrier, LigatureClass IGeneral and plastic surgeryContract manufacturingDec 11, 2020
KGCTube, Gastro-EnterostomyClass IIGastroenterology and urologyContract manufacturingMay 30, 2014
LXHOrthopedic Manual Surgical InstrumentClass IOrthopedicContract manufacturingApr 16, 2026
MUUSystem, Suction, LipoplastyClass IIGeneral and plastic surgeryContract manufacturingDec 11, 2020
NBHAccessories, ArthroscopicClass IOrthopedicContract manufacturingApr 16, 2026
ORGPlatelet And Plasma Separator For Bone Graft HandlingClass IIHematologyContract manufacturingNov 27, 2024
QAIPowered Microneedle DeviceClass IIGeneral and plastic surgeryContract manufacturingNov 26, 2024
QPBSystem, Suction, Lipoplasty For RemovalClass IIGeneral and plastic surgeryContract manufacturingDec 11, 2020